Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/30—Inkjet printing inks
  • C09D11/32—Inkjet printing inks characterised by colouring agents
  • C09D11/328—Inkjet printing inks characterised by colouring agents characterised by dyes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
  • C09B31/02—Disazo dyes
  • C09B31/08—Disazo dyes from a coupling component "C" containing directive hydroxyl and amino groups
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
  • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
  • C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
  • C09B67/0046—Mixtures of two or more azo dyes
  • C09B67/0055—Mixtures of two or more disazo dyes

Definitions

• This invention relates to anionic dyes and inks, and particularly black anionic dyes which have differential water-solubility dependent upon pH.
• B is 3-carboxyphenyl because this compound shows a particularly deep black shade and negligable bronzing when printed on plain paper.
• the compound of the present invention is useful as a colorant either alone or in admixture with another compound to form a composition.
• a preferred composition comprises a first compound according to the first aspect of the present invention and a second compound of Formula (1) wherein B is 3- or 4- carboxyphenyl and X is sulpho at the 6- or 7- position. It is preferred that the first and second compound are present in a weight-to-weight ratio of 95:5 to 5:95, more preferably 80:20 to 20:80, especially 40:60 to 60:40.
• the preferred compounds of Formula (1) and compositions, hereinafter collectively referred to as dyes, are in the form of a salt with a cation or mixture of cations, for example in the form of an alkali metal, ammonium or optionally substituted lower alkyl ammonium salt.
• the cation is preferably ammonium or optionally substituted lower (ie, C1 ⁇ 4-) alkyl ammonium, although when B is 3-carboxyphenyl the cation can be an alkali metal such as sodium.
• a preferred optional substituent which may be present on the optional substituted lower alkyl ammonium cations is a hydroxy group.
• Especially preferred cations are ammonium, mono-, di-, tri- and tetra-(C1 ⁇ 4-alkyl)ammonium and mono-, di-, tri- and tetra- (hydroxy-C1 ⁇ 4-alkyl)ammonium. It is, however, most preferred that the dyes are in the form of an ammonium (ie, NH4+) or mixed ammonium and alkali metal (especially sodium) salt.
• optionally substituted lower alkylammonium cations include methylammonium, ethylammonium, dimethylammonium, diethylammonium, trimethyammonium, triethylammonium, tetramethylammonium and tri(2-hydroxyethyl)ammonium.
• the compounds according to the first aspect of the present invention can be made by diazotising 3- or 4-carboxyaniline and coupling with alpha-naphthylamine to give a monoazo compound, diazotising the resultant monoazo compound and coupling with gamma acid.
• the dyes of the present invention can be converted into their ammonium or optionally substituted lower alkylammonium salt by dissolving the dye in the form of a salt with an alkali metal, acidifying with a mineral acid, adjusting the solution to pH 9-9.5 with ammonia or an optionally substituted lower alkylamine and removing alkali metal chloride ions by dialysis.
• the preferred dyes according to the invention are intended for use in ink jet printing.
• the dyes of the present invention are useful colorants for inks, and are notable for the good water fastness and the deep black shades with high optical density and minimal "bronzing" of their prints on plain paper.
• the dyes also have good solubility in aqueous media at a pH which causes little or no corrosion of the mechanism of ink jet printing devices.
• a suitable ink comprises a mixture of one or more compounds according to the first aspect of the present invention or a composition as hereinbefore described and a liquid medium, preferably an aqueous medium, for example an ink analogous to those described in US patent specification 4,963,189. It is preferred that the compound, compounds or composition are completely dissolved in the liquid medium to form a solution.
• the ink preferably contains from 0.5% to 20%, more preferably from 0.5% to 15%, and especially from 1% to 5%, by weight of the dye based on the total weight of the ink.
• the liquid medium is preferably water or a mixture comprising water and a water-soluble organic solvent, preferably respectively in a weight-to-weight ratio of 99:1 to 1:99, more preferably 95:1 to 50:50, especially 90:10 to 60:40.
• the water-soluble organic solvent is preferably a C1-C4-alkanol such as methanol, ethanol, n-propanol, isopropanol, n-butanol, sec-butanol, tert-butanol or isobutanol; an amide such as dimethylformamide or dimethylacetamide; a ketone or ketone alcohol such as acetone or diacetone alcohol; an ether such as tetrahydrofuran or dioxane; a polyalkylene glycol such as polyethylene glycol or polypropylene glycol; an alkylene glycol or thioglycol containing a C2-C6 alkylene group such as ethylene glycol, propylene glycol, butylene glycol or triethylene glycol; a thiodiglycol, hexylene glycol, or diethylene glycol; a polyol such as glycerol or 1,2,6-hexanetriol; a lower al
• the preferred water-soluble organic solvent is an alkylene glycol or lower alkyl ether of a polyhydric alcohol such as ethylene glycol, diethylene glycol, triethylene glycol or 2-methoxy-2-ethoxy-2-ethoxyethanol; or a polyethylene glycol with a molecular weight of up to 500.
• a preferred specific solvent mixtures is a binary mixture of water and diethylene glycol in a weight-to-weight ratio as mentioned above.
• the ink of the present invention contains a penetrant which assists permeation of the compound into a substrate such as paper and optionally up to 0.5% by weight of sodium borate.
• a further aspect of the present invention provides a process for printing a substrate with an ink using an ink jet printer, characterised in that the ink contains at least one compound according to the first aspect of the present invention or a composition as hereinbefore described.
• a suitable process for the application of an ink according to the invention to a substrate comprises forming the ink into small droplets by ejection from a reservoir through a small orifice so that the droplets of ink are directed at the substrate; this process is commonly referred to as ink jet printing, and the preferred processes for application of the inks hereinbefore defined are piezoelectric ink jet printing, and in particular thermal ink jet printing.
• thermal ink jet printing programmed pulses of heat are applied to the ink adjacent to the orifice during relative movement between the substrate and the reservoir.
• the preferred substrate is a cellulosic substrate, especially paper.
• the type of ink jet printer is not believed to be critical; however, it is preferably a thermal ink jet printer.
• the preferred ink used in the process is as hereinbefore described.
• paper printed with a compound, composition or ink according to the invention is provided.
• Dye A 1-hydroxy-2-(4-[3-carboxyphenyl-azo]-7-sulphonaphth-1-ylazo)-3-sulpho-7-aminonaphthalene, hereinafter referred to as Dye A, was prepared as follows
• 3-Aminobenzoic acid (13.7g, 0.1M) was stirred in water (150ml) at room temperature and 2N NaOH added to form a solution at pH 8.0.
• 2N NaNO2 solution 50ml was added and the mixture stirred to homogenise.
• the solution was added gradually to a mixture of ice/water (150ml) and 35% HCl (50ml) at 5°C and the resulting suspension stirred for 2 hours at 50°C.
• Sulphamic acid solution (10%) was added in order to remove excess nitrous acid and give a diazo solution.
• 1,7-Cleves acid (22.3g, 0.1M) was dissolved in a solution of water (150ml) and 32% NaOH solution at pH 8.5, and the solution cooled to 10°C.
• To this solution was added the above diazo solution and the pH raised to 5.5 by the addition of Na2CO3 solution (20%) to give an orange suspension which was stirred for 16 hours at 10°C, before raising the pH to 7.0 by addition of 2N NaOH solution and heating at 70°C.
• 25% NaCl aqueous (w/v) was added and the precipitated dye collected by filtration and washed with NaCl aqueous solution (25%, 200ml) to give a paste.
• the paste from Stage 1 was dissolved in water (100ml) and 2N NaOH solution at pH 9.0. 2N NaNO2 solution (50ml) was added and the mixture stirred for 3 minutes, then added gradually to a mixture of ice/water (150ml) and 36% HCl (50ml) at 5°C using rapid agitation. The resulting suspension was stirred for 1 hour at 5°C. Sulphamic acid solution (10%) was added in order to remove excess nitrous acid and gave a diazo suspension.
• Gamma acid (26.5g, 0.1M) was dissolved in water (150ml) and 2N NaOH solution at pH 9.0. Na2CO3 (10g) was added and the solution cooled to 0-10°C.
• 3-Aminobenzoic acid (13.7g, 0.1M) was diazotised by the method described in the preparation of Dye A, Stage 1, to give a diazo solution.
• the paste from Stage 1 (0.1M) was diazotised and coupled with gamma acid by a method analogous to that described in the preparation of Dye A, Stage 2, to give the disodium salt of 1-hydroxy-2-(4-[3-carboxyphenylazo]-naphth-1-ylazo)-3-sulpho-7-amino- naphthalene.
• ink Dye from Stage No. (parts) Liquid medium and other components (parts) 1 2 (2.5) Water (60) Ethylene glycol (40) 2 2 (4.0) Water (85) Diethylene glycol (15) 3 2 (5.0) Water (90) Diethylene glycol (10) 4 2 (3.0) Water (65) Glycerol (25) Triethanolamine (10) 5 2 (2.0) Water (80) Dye A (2.0) Ethylene glycol (15) Polyethylene glycol (MW 200) (5) 6 2 (2.2) Water (89.8) 2-Pyrrolidone (10) Sodium Borate (0.2)
• the printed image obtained has high resistance to water and gives a deep black shade showing little or no bronzing.
• the paste was stirred in water (300ml) and conc.ammonium hydroxide added to raise the pH to 9-9.5.
• the solution was then dialysed to remove chloride ions and solvent evaporated to give the mixed ammonium-sodium salt.
• the printed image When made into an ink and printed onto plain paper using a thermal ink jet printing machine, the printed image has a very high resistance to water with deep black shades showing little bronzing.
• the disodium salt of 1-hydroxy-2-(4-[3-carboxyphenylazo]naphth-1-ylazo)-3-sulpho-7-aminonaphthalene, prepared according to the method of Example 1 was converted to the mixed ammonium-sodium salt by a method analogous to that described in Example 2.
• the printed image obtained When converted to an ink and printed onto plain paper using a thermal ink jet printing machine the printed image obtained has very high water fastness and a deep black shades showing negligible bronzing.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Inks, Pencil-Leads, Or Crayons (AREA)
• Paper (AREA)

Applications Claiming Priority (2)

Publications (2)

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Family Applications (1)

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Cited By (4)

Citations (3)

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• 1991
  • 1991-01-08 GB GB919100302A patent/GB9100302D0/en active Pending
  • 1991-12-16 EP EP91311668A patent/EP0494522B1/de not_active Expired - Lifetime
  • 1991-12-16 DE DE69116121T patent/DE69116121T2/de not_active Expired - Fee Related
• 1992
  • 1992-01-03 US US07/816,677 patent/US5254675A/en not_active Expired - Lifetime
  • 1992-01-07 JP JP04000567A patent/JP3105323B2/ja not_active Expired - Fee Related

Patent Citations (3)

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